Job Summary:
The Clinical Research Project Coordinator (CRPC) will work closely with study team in the iOUCH Pain Lab at The Hospital for Sick Children to assist with the coordination of various studies (e.g. participant recruitment, data collection, data entry). The Clinical Research Project Coordinator will also work closely with the research team and reports to the Principal Investigator or her designate (i.e., Project Manager).
Project Summary:
Through evidence-based research and knowledge translation processes, the iOUCH Lab at The Hospital for Sick Children aims to improve the lives of children and adolescents through the use of innovative information and communication technologies.
Here's what you get to do:
The CRPC will assist with the coordination of several clinical research studies related to chronic pain and other painful conditions. These projects include the evaluation of an online self-management program for adolescents with neurofibromatosis, validation testing of a new tool to screen for risk of chronic post-surgical pain, qualitative analysis of pain experiences after cancer, management of the Canadian Pediatric Chronic Pain Registry, and other lab projects as needed.
Specific job duties include:
- Study set-up, including obtaining and maintain research ethics approval, research ethics amendments
- Participate in study recruitment, consenting, participant follow-up, and data collection.
- Responsible for study coordination across all participating sites.
- Oversee and participate in data management (e.g., data cleaning and data entry) and quantitative/qualitative data analysis.
- Assist with manuscript preparation.
- Participate in other administrative activities to ensure the smooth running of both projects.
Here's what you need:
- Post-Secondary degree in a Health Science discipline.
- Minimum of two years experience in clinical research.
- Previous clinical trial experience is essential.
- Familiarity with both quantitative and qualitative research methodology including conducting interviews and analyzing quantitative and qualitative data
- Previous experience working with quantitative (e.g., SAS) and qualitative (e.g., NVivo) software is an asset.
- Previous experience with online databases (e.g., REDCap)
- Experience in a pediatric clinical research experience is an asset
- Superior communication, organization and time management skills.
- Ability to develop strong working relationships.
- A commitment to understanding and aiding in the pursuit of equity, diveristy and inclusion objectives.
Employment Type: 1 year, 1.0 FTE Temporary contract
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